Search results for "Click reaction"

showing 4 items of 4 documents

Strain-Promoted Cycloaddition of Cyclopropenes with o-Quinones : A Rapid Click Reaction

2018

Abstract Novel click reactions are of continued interest in fields as diverse as bio‐conjugation, polymer science and surface chemistry. Qualification as a proper “click” reaction requires stringent criteria, including fast kinetics and high conversion, to be met. Herein, we report a novel strain‐promoted cycloaddition between cyclopropenes and o‐quinones in solution and on a surface. We demonstrate the “click character” of the reaction in solution and on surfaces for both monolayer and polymer brush functionalization.

KineticsClick Chemistry | Hot Paper010402 general chemistryPolymer brushO quinones01 natural sciencesCatalysisReaccions químiquesMonolayerotorhinolaryngologic diseasesMetal-free click reactionsVLAGchemistry.chemical_classificationMonolayersMass spectrometry010405 organic chemistryChemistryCommunicationOrganic ChemistryGeneral MedicineGeneral ChemistryPolymerCombinatorial chemistryOrganische ChemieCycloadditionCommunications0104 chemical sciencesKineticsClick chemistrySurface modificationPolymer brushesQuímica orgànicahuman activitiesAngewandte Chemie - International Edition
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Combining Spontaneous Polymerization and Click Reactions for the Synthesis of Polymer Brushes: A "Grafting Onto" Approach

2013

Two novel benzofulvene monomers bearing propargyl or allyl groups have been synthesized by means of readily accessible reactions, and were found to polymerize spontaneously by solvent removal, in the apparent absence of catalysts or initiators, to give the corresponding polybenzofulvene derivatives bearing clickable propargyl or allyl moieties. The clickable propargyl and allyl groups were exploited in appropriate click reactions to develop a powerful and versatile "grafting onto" synthetic methodology for obtaining tailored polymer brushes.

Magnetic Resonance Spectroscopypolymerclick reactionsCyclopentanesCatalysisCatalysisPolymerizationchemistry.chemical_compoundMolecular recognitionphotograftingPolymer chemistryClick reactionpolymerschemistry.chemical_classificationorganic chemicalsOrganic Chemistryfood and beveragesGeneral ChemistryPolymerGraftingMonomerchemistryPolymerizationpontaneous polymerizationPropargylPhotograftingSolventsClick Chemistrymolecular recognition
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A recent portrait of bioactive triazoles

2010

Scientists have extensively explored new synthetic routes in order to obtain 1,2,3- and 1,2,4-triazoles as they represent a very interesting class of compounds due to their wide range of biological activities such as antitumor, antiinflammatory, analgesic, antifungal, antibacterial, antiviral, etc. This mini review reports the synthesis and the biological activities of compounds containing a triazole moiety published since 2007. No attempt is made to provide a comprehensive literature overview, our aim is to highlight some more recent examples of synthetic biological active compounds. In particular, we focus on the applications of “click reactions” that allow the regioselective synthesis of…

PortraitChemistryArt historySettore CHIM/06 - Chimica OrganicaGeneral Pharmacology Toxicology and PharmaceuticsAntibacterial antifungal antitumor antiviral click reaction enzyme-inhibitor triazole
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MODIFICATION OF HYDROPHOBIC SURFACE WITH POLYASPARTAMIDE-BASED POLYCATIONS FOR BIOMEDICAL APPLICATION

2013

A convenient way for the achievement of polymer-based solid materials for specific biomedical applications is grafting the appropriate macromolecules onto the surfaces in order to confer them specific properties. To date many approaches have been used to covalently modify polymeric surfaces, and among them chemoselective coupling reactions, usually referred as “click” reactions, gained much attention thanks to simple procedure with high reaction rate under mild reaction conditions (at normal temperature and pressure) [1]. In particular, radical-initiated thiol-yne “photo-click” chemistry has been demonstrated as an effective way to functionalize efficiently surfaces. This method gives also …

thiol-yne click reactionPHEA; lipoic acid; antibacterial PLA surfaces; thiol-yne click reaction.antibacterial PLA surfacesSettore CHIM/09 - Farmaceutico Tecnologico ApplicativoPHEA lipoic acid antibacterial PLA surfaces thiol-yne click reaction.PHEAlipoic acid
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